Introduction:Basic information about Dibenz[b,f]azepine-5-carbonyl chloride CAS 33948-22-0, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Dibenz[b,f]azepine-5-carbonyl chloride Basic information
| Product Name: | Dibenz[b,f]azepine-5-carbonyl chloride |
| Synonyms: | CHLOROCARBONYL LIMINOSTILBEN;DIBENZ [B,F]AZEPINE-5-CARBONYL CHLORIDE;IMINOSTILBENE-5-CARBONYL CHLORIDE;IMINOSTILBENE CARBONYL CHLORIDE;5-chlorocarbonyl iminostilbene;5H-DIBENZ[B,F]AZEPINE-5-CARBONYL CHLORIDE;5-(Chlorocarbonyl)-5H-dibenzo[b,f]azepine;N-Chlorocarbonyliminostilbene |
| CAS: | 33948-22-0 |
| MF: | C15H10ClNO |
| MW: | 255.7 |
| EINECS: | 412-100-5 |
| Product Categories: | Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks;N-Containing;Others;Heterocyclic Building Blocks;Aromatics;Heterocycles;Intermediates;Intermediates & Fine Chemicals;Pharmaceuticals |
| Mol File: | 33948-22-0.mol |
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Dibenz[b,f]azepine-5-carbonyl chloride Chemical Properties
| Melting point | 149-153 °C (lit.) |
| Boiling point | 413.7±38.0 °C(Predicted) |
| density | 1.316±0.06 g/cm3(Predicted) |
| storage temp. | 2-8°C |
| solubility | soluble in Chloroform, Dichloromethane, Ethyl Acetate |
| form | Oil |
| pka | -3.69±0.20(Predicted) |
| color | Brown |
| InChI | InChI=1S/C15H10ClNO/c16-15(18)17-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)17/h1-10H |
| InChIKey | APJYHXJGXDPGBA-UHFFFAOYSA-N |
| SMILES | C(Cl)(N1C2=CC=CC=C2C=CC2=CC=CC=C12)=O |
| CAS DataBase Reference | 33948-22-0(CAS DataBase Reference) |
Safety Information
| Hazard Codes | C |
| Risk Statements | 34 |
| Safety Statements | 26-36/37/39-45 |
| RIDADR | UN 3261 8/PG 2 |
| WGK Germany | 3 |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| Hazard Classifications | Skin Corr. 1B |
Dibenz[b,f]azepine-5-carbonyl chloride Usage And Synthesis
| Chemical Properties | Pink Solid |
| Uses | Dibenz [b,f]azepine-5-carbonyl chloride may be used in the preparation of trans-10,11-dibromo-10,11-dihydro-5H-dibenz[b,f]azepine-5-carbonyl chloride via bromination using bromine. It may also be used to prepare urea derivatives, which are potent P2X4 receptor (purinergic receptor) antagonists. |
| Uses | An intermediate in the preparation of Carbamazepine. |
| General Description | Dibenz [b,f]azepine-5-carbonyl chloride or 5H-dibenz [b,f]azepine-5-carbonyl chloride is a tricyclic heterocyclic compound that can be synthesized from 5H-dibenz[ b,f]azepine. |
Dibenz[b,f]azepine-5-carbonyl chloride Preparation Products And Raw materials
| Raw materials | Iron-->Sodium Methoxide-->2-Nitrotoluene-->Iminostilbene-->2,2'-ETHYLENEDIANILINE |